74372-80-8

Upstream product

• 3162-96-7 methyl 4,6-O-benzylidene-α-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 74372-81-9 methyl 2,3-di-O-benzyl-6-O-trityl-α-D-arabino-hexopyranosid-4-ulose 
• 33164-03-3 methyl 2,3-di-O-benzyl-α-D-altropyranoside 
• 76-83-5 trityl chloride 
• 7177-79-9 methyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 

Downstream Products

• 37116-67-9 methyl-(O²,O³-dibenzyl-O⁴-methyl-O⁶-trityl-α-D-glucopyranoside) 
• 87326-58-7 methyl 4-O-allyl-2,3-di-O-benzyl-6-O-trityl-α-D-glucopyranoside 
• 81255-12-1 methyl 2,3-di-O-benzyl-6-O-triphenylmethyl-α-D-xylo-hexopyranosid-4-ulose 
• 162191-09-5 Methyl 2,3-di-O-benzyl-4-deoxy-6-O-triphenylmethyl-α-D-xylo-hexopyranoside 
• 17791-36-5 methyl 2,3-di-O-benzyl-α-D-glucopyranoside 
• 71756-38-2 methyl 2,3-di-O-benzyl-6-O-trityl-α-D-galactopyranoside 
• 74024-29-6 methyl 4-O-allyl-2,3-di-O-benzyl-α-D-glucopyranoside 
• 200621-49-4 (1R,6R,8S,9R,10S)-9,10-bis(benzyloxy)-8-methoxy-2,7-dioxabicyclo[4.4.0]dec-4-ene 
• 200621-48-3 methyl 4-O-allyl-2,3-di-O-benzyl-6,7-dideoxy-α-D-gluco-hept-6-enopyranoside 
• 122079-92-9 1,6-di-O-acetyl-4-O-allyl-2,3-di-O-benzyl-α-D-glucopyranose 
• 74024-31-0 4-O-allyl-2,3-di-O-benzyl-1,6-di-O-(N-phenylcarbamoyl)-D-glucopyranose 
• 74024-31-0 4-O-allyl-2,3-di-O-benzyl-1,6-di-O-(N-phenylcarbamoyl)-α-D-glucopyranose 
• 1079963-50-0 methyl 2,3-di-O-benzyl-4-O-propargyl-6-O-trityl-α-D-glucopyranoside 
• 1380315-71-8 methyl 2,3-di-O-benzyl-6-O-(2-bromomethylbenzyl)-4-O-(4-methoxybenzyl)-α-D-glucopyranoside 

Relevant academic research and scientific papers

3-Butenyloxycarbonyl as a new hydroxyl protecting group in carbohydrate synthesis

3-Butenyloxycarbonyl (Bloc) has been identified as a new hydroxyl protecting group, which can be introduced under mild conditions in high yields and selectively removed by OsO4/NaIO4/2,6-lutidine in CH3CN-H2O wi

Intramolecular base-free sonogashira reaction for the synthesis of benzannulated chiral macrocycles embedded in carbohydrate templates

A base-free, intramolecular Sonogashira reaction-based general approach has been established for the diversity-oriented synthesis (DOS) of fused bi- and tricyclic systems containing benzannulated, 10- to 13-membered chiral macrocycles embedded in carbohydrate templates. Macrocycles with different ring sizes have been prepared by pre-designing the chiral building blocks. Base-sensitive groups like acetyl and TBDPS survived the reaction conditions. Copyright

Disaccharide-containing macrocycles by click chemistry and intramolecular glycosylation

In this study o- and m-xylylene moieties in combination with a triazolylmethyl moiety have been successfully employed as a relatively rigid spacer system in intramolecular glycosylation reactions. Phenyl 3,4,6-tri-O-benzyl-2-O-propargyl-1-thio-D-glucopyra